Literature DB >> 809492

Axonal projections and connections of the principal sensory trigeminal nucleus in the monkey.

R L Smith.   

Abstract

To date, anatomical studies of ascending principal sensory trigeminal nuclear (PrV) axons in the monkey have been restricted to few incomplete investigations utilizing the Marchi method. In the present study total or partial unilateral stereotaxic lesions of PrV were made in cebus and rhesus monkeys and analyzed with the aid of a variety of Nauta silver impregnation techniques applied to frozen sections. Analysis of the fiber degeneration emanating from PrV lesions indicates that PrV fibers form an ascending system composed of two distinct components. Most PrV axons project ventromedially from PrV through the ventral pontine tegmentum and gradually decussate across the midline in the mesencephalic tegmentum up to the level of the caudal pole of nucleus interpeduncularis. These decussated fibers form the trigeminal lemniscus, which courses dorsomedial to the medial lemniscus during its ascent into the diencephalon. A few whorls of preterminal fiber degeneration separating from the trigeminal lemniscus first appear in the magnocellular area of the thalamus medial to the medial geniculate body. The lemniscal PrV axons terminate densely throughout most, but not all, of the magnocellular part of nucleus ventralis posteromedialis (VPM) contralateral to the side of their origin. Some collateral-like fibers from the trigeminal lemniscus also were observed ending in the ventral segment of the zona incerta. Other axons, arising chiefly from the dorsal one-third of PrV form a smaller ipsilateral trigeminothalamic projection. These fibers all remain on the side of their origin and terminate consistently in a discrete dorsomedial paralaminar portion of VPM that does not receive lemniscal PrV connections. A commissural fiber system at the pontine level connects parvicellular reticular cells with their counterparts and the motor trigeminal nucleus of the opposite side. These interconnections appear to provide an anatomical link for the integration of bilateral trigeminal sensory information and motor function.

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Year:  1975        PMID: 809492     DOI: 10.1002/cne.901630307

Source DB:  PubMed          Journal:  J Comp Neurol        ISSN: 0021-9967            Impact factor:   3.215


  6 in total

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Authors:  E G Jones; H D Schwark; P A Callahan
Journal:  Exp Brain Res       Date:  1986       Impact factor: 1.972

2.  The role of the trigeminal sensory nuclear complex in the pathophysiology of craniocervical dystonia.

Authors:  Lynley Bradnam; Christine Barry
Journal:  J Neurosci       Date:  2013-11-20       Impact factor: 6.167

3.  Response properties of temporomandibular joint mechanosensitive neurons in the trigeminal sensory complex of the rabbit.

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Journal:  Exp Brain Res       Date:  2012-08-02       Impact factor: 1.972

4.  Electroacupuncture Plus Auricular Acupressure for Chemotherapy-Associated Insomnia in Breast Cancer Patients: A Pilot Randomized Controlled Trial.

Authors:  Jialing Zhang; Zongshi Qin; Tsz Him So; Haiyong Chen; Wing Lok Lam; Lo Lo Yam; Pui Yan Chan; Lixing Lao; Zhang-Jin Zhang
Journal:  Integr Cancer Ther       Date:  2021 Jan-Dec       Impact factor: 3.279

5.  New Insights in Trigeminal Anatomy: A Double Orofacial Tract for Nociceptive Input.

Authors:  Dylan J H A Henssen; Erkan Kurt; Tamas Kozicz; Robert van Dongen; Ronald H M A Bartels; Anne-Marie van Cappellen van Walsum
Journal:  Front Neuroanat       Date:  2016-05-10       Impact factor: 3.856

6.  Morphology and connections of intratrigeminal cells and axons in the macaque monkey.

Authors:  Susan Warren; Paul J May
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  6 in total

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